Compartmentalization of recombinant polypeptides in host cells

ABSTRACT

The present invention relates to host cells which contain at least two functional recombinant polypeptides, at least one of which is bound to a support, preferably in each case in different cell compartments, for example cytosol, cytoplasmic membrane, periplasm and outer membrane, and also to methods for preparing said host cells. The cells of the invention are particularly, suited as bioreactors for carrying out enzymatic reaction cascades for which compartmentalization of individual enzymes is advantageous or necessary.

The present invention relates to host cells which contain at least two functional recombinant polypeptides, at least one of which is bound to a support, preferably in each case in different cell compartments, e.g. cytosol, cytoplasmic membrane, periplasm and outer membrane, and also to methods for preparing said host cells. The cells of the invention are particularly suited as bioreactors for carrying out enzymatic reaction cascades for which compartmentalization of individual enzymes is advantageous or necessary.

The use of living cells as “enzyme reactors” for preparing biological substances, e.g. polyhydroxy fatty acids, is of great importance for the biotechnological industry. To this end, it is common to introduce foreign genes into a host cell and to express said genes, in order to obtain in this manner a host cell with recombinant enzymes, which is capable of synthesizing a desired product. A disadvantage of known methods, however, was that the enzymes generated in the host cells by expression of the foreign genes were not stable, had too little activity or were present in too small an amount. Particular difficulties also stepped when carrying out multistage reactions in which substrates or products of one stage may have an adverse effect on other stages.

It was an object of the present invention to eliminate at least partially the problems of the prior art and to provide host cells which are capable of presenting functional recombinant polypeptides in a stable form and, in particular, of carrying out multistage enzyme reactions.

The object is achieved by providing a host cell comprising at least two functional recombinant polypeptides at least one of which is bound to a support.

Surprisingly, it was found that support-bound recombinant expression of heterologous polypeptides preferably in different compartments of a cell, e.g. of Gram-negative bacterial cells or of eukaryotic cells, leads to stable presentation of the heterologous polypeptides in a functional (i.e. immunologically or/and biologically, e.g. enzymatically, active) form. If the host cell is a Gram-negative bacterial cell, the cell compartments may preferably be selected from the cytosol, the cytoplasmic membrane (outside and inside), the periplasmic space and the outer membrane (outside and inside). If the host cell is a eukaryotic cell, said compartments may preferably be selected from the cytosol, the cytoplasmic membrane (outside and inside) and cell organelles such as, for example, Golgi, lysosomes, mitochondria, chloroplasts, vacuoles or endoplasmic reticulum.

The functional recombinant proteins present in the host cell are preferably cooperative, i.e. they fulfill a common immunological or/and biological function, for example as enzymes in a multistage reaction cascade.

At least one, preferably a plurality, of the functional recombinant polypeptides is bound to a support, for example in the form of fusion polypeptides, and contain at least one functional domain and at least one support domain. Preferred forms of support-bound polypeptides are S-layer structures (fusion polypeptides with S-layer support domains), membrane-bound polypeptides (fusion polypeptides with membrane-integrated support domains) or/and components of recombinant phage structures. If it is desired to export the functional polypeptides from the cytosol to other cell compartments, said polypeptides are expressed together with suitable targeting domains which facilitate export to the cell compartment desired in each case. Examples of targeting domains are signalpeptide or/and helper sequences which facilitate passage through the membranes.

In a preferred embodiment of the invention, at least one of the support-bound polypeptides is present as recombinant S-layer structure. S-layers are crystalline bacterial cell surface proteins which are composed of identical self-assembled units. Genetic data and sequence information for various S-layer genes from microorganisms can be formed, for example, in Peyret et al. (Mol. Microbiol. 9 (1993), 97-109). These data are expressly incorporated by reference.

Preferred S-layer genes are the B.stearothermophilus PV72 genes sbsA and sbsB. The sequences of these genes can be found, for example, in the international patent application PCT/EP97/00432 which also discloses production of a recombinant S-layer fusion protein in the cytoplasm of Gram-negative host cells. The international patent application PCT/EP98/04723 in turn describes production of a recombinant S-layer protein in various compartments of Gram-negative bacteria cells or eukaryotic cells. Regarding the construction of recombinant S-layer genes and production of suitable expression constructs, these two said international applications are expressly referred to. However, no indication of coexpression of two different functional recombinant polypeptides is found there.

Surprisingly, it was found that it is possible to co-express simultaneously or/and sequentially a plurality of recombinant S-layer proteins, where appropriate in combination with further heterologous proteins, for example in various compartments of host cells, in particular of Gram-negative bacterial cells and eukaryotic cells.

The nucleotide sequence of the gene coding for the mature SbsA protein is indicated from position 91-3684 in SEQ ID No. 1. The corresponding amino acid sequence is depicted in SEQ ID No. 2. The nucleotide sequence of the gene coding for the mature SbsB protein is indicated from position 94-2763 in SEQ ID No. 3. The corresponding amino acid sequence is depicted in SEQ ID No. 4.

In a first preferred embodiment (sbsA), the nucleic acid coding for the support domain of a functional peptide is selected from

(i) a nucleic acid which comprises the nucleotide sequence from position 91 to 3684 shown in SEQ ID No. 1,

(ii) a nucleic acid which comprises a nucleotide sequence corresponding to the nucleic acid from (i) within the framework of the degeneracy of the genetic code, and

(iii) a nucleic acid which comprises a nucleotide sequence hybridizing with the nucleic acids from (i) or/and (ii) under stringent conditions.

In a second preferred embodiment (sbsB), the nucleic. acid coding for the support domain of a functional peptide is selected from

(i) a nucleic acid which comprises the nucleotide sequence from position 94 to 2763 shown in SEQ ID No. 3,

(ii) a nucleic acid which comprises a nucleotide sequence corresponding to the nucleic acid from (i) within the framework of the degeneracy of the genetic code, and

(iii) a nucleic acid which comprises a nucleotide sequence hybridizing with the nucleic acids from (i) or/and (ii) under stringent conditions.

“Stringent hybridization” in accordance with the present invention means that hybridization still occurs even after washing at 55° C., preferably 60° C., in an aqueous low-salt buffer (e.g. 0.2×SSC) (see also Sambrook et al. (1989), Molecular Cloning. A Laboratory Manual).

Preferred sites for inserting peptide- or polypeptide-coding sequences into the sbsA gene are regions between positions 200-3600 of the nucleotide sequence shown in SEQ ID No. 1. Particularly preferred insertion sites are the NruI cleavage site at position 585, the PvuII cleavage site at position 881, the SnaB I cleavage site at position 920, the PvuII cleavage site at position 2507 and the PvuII cleavage site at position 2652 (PCT/EP 97/00 432). Further preferred insertion sites are positions 562, 1087, 1813, 1947, 2295, 2652, 3046, 3484 and 3594. The positions indicated in each case refer to the first nucleotide of the insertion.

Preferred sites of insertion into the sbsB gene are regions between positions 200-2600 of the nucleotide sequence shown in SEQ ID No. 3. Particularly preferred insertion sites are positions 410 (codon 136), 484 (codon 161/162) and 1583 (codon 528/529) (PCT/EP 97/00432). Further preferred insertion sites are positions 598, 1012, 1435, 1808 and 2301, the position indicated in each case referring to the first nucleotide of the insertion.

Alternatively or additionally, it is also possible to produce support-bound polypeptides in a different form, for example as components of recombinant phage structures, e.g. øX174 or øCH1.

Yet another possibility of producing support-bound polypeptides is the synthesis as fusion polypeptides with membrane integration domains so that the functional polypeptides are located at the locations desired in each case (outside or inside of a membrane chosen in each case).

The support sequence used for integration into the outer membrane of prokaryotic Gram-negative host cells may be the C-terminal domain of IgA protease from Neisseria or Haemophilus (Klauser et al., J. Mol. Bio. 23.4 (1993), 579-593). Further suitable support domain sequences are OmpA or LamB sequences or parts thereof ( . . . ).

For integration into the cytoplasmic membrane of Gram-negative prokaryotic host cells, preference is given to using a hydrophobic nonlytical membrane-integrating protein domain which has an α-helical structure. Examples of DNA sequences coding for such a membrane-integrating protein domain are described in the European patent 0 516 655.

For secretion into the periplasm of Gram-negative prokaryotic cells it is possible to use, for example, the malE signal peptide sequence. Other sequences which cause secretion into the periplasm are described, for example, in Blondel and Bedouelle (Eur. J. Biochem 193 (1990), 325-330; Adip-Conquy et al. (Protein Eng. 8 (1995), 859-863); Weller et al (Eur. J. Biochem. 236 (1996), 34-39) and Dubreuil et al. (FEMS Immunol. Med. Microbiol. 13 (1996), 317-323).

Known signal peptides for expression in the cytoplasmic membrane or in organelles of eukaryotic cells are the N-terminal transit peptide of plastocyanin for transport into chloroplasts (Weisbeek et al., J. Cell. Sci. Suppl. 11 (1989), 199-223), mitochondrial signal peptides for transport into mitochondria (Skerjanc, Biochem. Cell. Biol. 68 (1990), 9-16), targeting sequences for transport into vacuoles (Vitale and Chrispeels, Bioessays 14 (1992), 151-160), targeting sequences for the cell membrane, cytoplasm and Golgi apparatus (Stanley, Mol. Membr. Biol. 13 (1996), 19-27), retention signals for the endoplasmic reticulum (Lencer et al., J. Cell. Biol. 131 (1995),:951-962) and transfer sequences for the Golgi apparatus or the plasma membrane (Rambourg et al., Anat. Rec. 245 (1996), 447-458).

It is possible for the DNA sequence coding for the foreign polypeptide to contain, in addition to the segment coding for the signal peptide, one or more further segments coding for further protein domains. Such a segment may preferably be located between the segment coding for the signal peptide and the segment coding for the foreign polypeptide. This segment preferably codes for a secretory polypeptide from Gram-negative bacterial or eukaryotic organisms or a part thereof. A preferred example of such a nucleic acid segment is the malE gene which encodes maltose binding protein.

The foreign polypeptides are preferably selected from DNA-binding epitopes, antigenic, allergenic or immunogenic epitopes, metal-binding epitopes, stretavidin, enzymes, cytokines or antibody-binding proteins.

A preferred example is stretavidin which is suitable for docking biotinylated reagents, e.g. after integration into the outer membrane. Another preferred example is antigenic, allergenic or immunogenic epitopes, for example epitopes from pathogenic microorganisms such as, for example, bacteria, fungi, parasites etc., and viruses, or epitopes from plants or epitopes against endogenous substances, e.g. cytokines, and also against toxins, in particular endotoxins. Particularly preferred examples of immunogenic epitopes are epitopes from viruses, for example from herpesviruses such as, e.g., herpesvirus 1, e.g. glykoprotein Δ, herpesvirus 6 or pseudorabies virus (Lomniczi et al., J. Virol. 49 (1984), 970-979), in particular epitopes from the gB, gC or/and gD genes, epitopes from foot-and-mouth disease virus (FMDV), in particular epitopes from the gene segments coding for VP1, VP2 or/and VP3, epitopes from flaviviruses or epitopes from filoviruses such as, for example, Ebola, Marburg or Lassa virus. The immunogenic epitopes may be selected such that they promote generation of an antibody-mediated immune reaction or/and promote generation of a cellular immune reaction, for example by stimulation of T cells. Examples of suitable allergenic epitopes are birch pollen allergens, e.g. Bet v I (Ebner et al., J. Immunol. 150 (1993) 1047-1054). Particular preference is furthermore given to antigenic epitopes which are capable of binding and filtering out endogenous or exogenous substances such as, for example, cytokines or toxins from serum or other body fluids. Epitopes of this kind may include components of cytokine or toxin receptors or of antibodies against cytokines or toxins.

Modified foreign polypeptides, for example S-layer proteins; which have immunogenic or/and antigenic epitopes with glycosylation sites, are preferably produced in eukaryotic host cells in which glycosylation is possible. In this connection it is also possible to glycosylate the natural S-layer sequences. Examples of potential N-glycosylation sites in the S-layer gene sbsA are amino acid positions 26, 285, 343, 384, 387, 388, 418, 421, 483, 653, 675, 902, 924, 1048, 1058, 1118, 1154 and 1161. A potential N-glycosylation in the sbsB gene can occur in positions 155, 184, 213, 302, 303, 400, 463, 606, 755 and 915. Further possible modifications of the sbsA gene include amidation, phosphorylation by casein kinase II, N-myristoylation and phosphorylation by protein kinase C. Further possible modifications of the sbsB gene include phosphorylation by CAMP and cGMP-dependent protein kinase, phosphorylation by casein kinase II, N-myristoylation, phosphorylation by protein kinase C and attachment to a fibronectin receptor (via sequence RGD).

Likewise preferred foreign polypeptides are cytokines such as, for example interleukines, interferons or tumor necrosis factors. These molecules may be used, for example, in combination with immunogenic epitopes for the production of vaccines. In addition, antibody-binding proteins such as, for example, protein A or protein G, or DNA- or/and metal-binding epitopes such as, for example, leucine zipper, zinc finger, etc are also preferred.

The recombinant polypeptides are particularly preferably enzymes, in particular enzymes which catalyze a multistage enzymatic reaction. Specific examples are enzymes for the synthesis of polyhydroxyalkanoates, e.g. polyhydroxybutyric acid synthase (Lubitz and Resch, DE 44 171 69 A1; Slater, S. C., Voige W. H., Dennis, A. E. J. Bacteriol. (1998), 170:4431).

The present invention still further relates to recombinant bacterial ghosts obtainable from a Gram-negative host cell of the invention, which has at least two functional recombinant polypeptides bound to a support.

The preparation of suitable “bacterial ghosts” is described, for example, in the international patent application PCT/EP91/00967 which is hereby incorporated by reference. Said patent application discloses modified bacteria obtainable by transformation of a Gram-negative bacterium with the gene of a lytic membrane protein from bacteriophages, with the gene of a lytic toxin-releasing protein or with genes which contain part sequences thereof coding for lytic proteins, culturing of the bacterium, expression of this lysis gene and isolation of the resulting bacterial ghost from the culture medium.

As described in the European patent 0 516 655, the membrane of these bacteria may have bound to it a recombinant protein which is obtainable by expression of a recombinant DNA in these Gram-negative bacteria. This recombinant DNA comprises a first DNA sequence which codes for a hydrophobic, nonlytic membrane-integrating protein domain which has an α-helical structure and consists of 14-20 amino acids which may be flanked N- and C-terminally by in each case 2-30 amino acids of any kind. This first DNA sequence is operatively linked to a second DNA sequence which codes for a desired recombinant protein. Furthermore, the Gram-negative bacterium contains a third DNA sequence which is controlled separately from the first and second DNA sequences and codes for a lytic membrane protein from bacteriophages or a lytic toxin-releasing protein or for lytic parts thereof. Expression and lysis of recombinant Gram-negative bacteria of this type produce so-called “bacterial ghosts” which contain an intact surface structure with immunogenic epitopes bound to the surface.

The preparation of host cells of the invention is preferably carried out by a method in which

(a) a host cell which has been transformed with at least two nucleic acids coding for recombinant polypeptides is provided, at least one of the nucleic acids being linked to a sequence coding for a support domain, in order to facilitate expression of the recombinant polypeptide in a support-bound form,

(b) the host cell is cultured under conditions which lead to expression of the nucleic acids and to a generation of the polypeptides encoded thereby in a functional form.

Furthermore, the nucleic acids coding for the recombinant polypeptides are preferably operatively linked to sequences which provide for localization of the recombinant polypeptides in each case in different compartments of the host cell.

When expressing the recombinant proteins in support-bound form as modified S-layers, it is in addition also possible to express genes in the cell which code for an unmodified S-layer protein. In this case, it is possible for the modified S-layer proteins to form an S-layer structure which is compatible with the unmodified S-layer proteins. An example of this embodiment of the method of the invention is an E.coli cell transformed with four S-layer genes, two of which are natural sbsA or sbsB genes and the other two are recombinant sbsA or sbsB genes.

The nucleic acids coding for the recombinant polypeptides are preferably located on recombinant vectors which contain at least one copy of the nucleic acid. The vectors used may be conventional prokaryotic or eukaryotic chromosomal or extrachromosomal vectors. Examples of such vectors are described in Sambrook et al., supra. The vectors contain the nucleic acids coding for the recombinant polypeptides, operatively linked to an expression control sequence active in the particular host cell. The expression control sequence particularly preferably comprises a controllable promoter. Examples of suitable prokaryotic promoters are the tac, lac, trp and λ promoters. Examples of suitable eukaryotic promoters are the SV40, CMV and metallothionein promoters. The at least two nucleic acids coding for heterologous polypeptides are particularly preferably expressed by using two different controllable promoters, for example two different temperature-sensitive λ promoters, as already described.

The recombinant host cells (living host cells or ghosts) are suitable for a multiplicity of applications. A use as vaccine or adjuvant is preferred, and in this case recombinant polypeptides are used which comprise immunogenic epitopes of pathogenic and/or endogenous immunostimulating polypeptides such as, for example, cytokines.

Particular preference is given to using the host cells or/and bacterial ghosts of the invention as enzyme reactors.

The present invention is furthermore illustrated by the following examples and figures, in which

SEQ ID NO. 1 shows the complete nucleotide sequence of the coding segment of the B.stearothermophilus S-layer gene sbsA;

SEQ ID NO. 2 shows the amino acid sequence derived therefrom;

SEQ ID NO. 3 shows the complete nucleotide sequence of the coding segment of the B.stearothermophilus S-layer gene sbsB;

SEQ ID NO. 4 shows the amino acid sequence derived therefrom.

FIG. 1 shows a diagrammatic representation of the possibilities for locating heterologous polypeptides in different compartments of a Gram-negative bacterial cell.

(a) A Gram-negative bacterial cell is composed of the cytoplasm (cy), the inner membrane (im), the periplasm (pp) and the outer membrane (om).

(b) Heterologous polypeptides can be exported to the periplasm by linkage with suitable targeting sequences (pe).

(c) Heterologous polypeptides can be anchored on the inside of the inner membrane (mae).

(d) In the periplasm, heterologous polypeptides can be immobilized in the form of recombinant S-layers (sie).

(e) Not only one but a plurality of species of recombinant heterologous polypeptides can be immobilized as S-layers in the periplasm.

FIG. 2 shows the diagrammatic representation of a recombinant bacterial cell of the invention, which contains various heterologous polypeptides (e.g. enzymes) in different compartments.

EXAMPLES 1. Bacteria Strains, Media and Plasmids

Gram-positive bacteria of Bacillus stearothermophilus PV72 strain were cultured at 58° C. in SVIII medium (Bartelmus and Perschak, Z.Zuckerind.7 (1957), 276-281). E.coli bacteria were cultured in LB medium (Sambrook et al., (1989), supra). For the selection of transformants, ampicillin was added to the medium at a final concentration of 100 μg/ml. The plasmid pPlcAT10 (λpL, bla, colE1) (Stanssens et al., Gene 36 (1985), 211-223) was used as cloning vector.

2. Manipulation of DNA Fragments

DNA restriction analysis, agarose gel electrophoresis and cloning of DNA fragments were carried out according to the standard methods described in Sambrook et al. (1989), supra.

Competent cells were transformed by electroporation using a Bio-Rad Gene Pulser (Bio-Rad Laboratories, Richmond, Calif., USA) following protocols of the manufacturer.

Plasmid DNA was isolated according to the method of Birnboim and Doly (Nucleic Acids Res.7 (1979), 1513-1523). Chromosomal DNA was isolated according to the methods described in Ausubel et al. (Current Protocols in Molecular Biology (1987), New York, John Wiley).

Restriction endonucleases and other enzymes were obtained from Boehringer Mannheim, New England Biolabs or Stratagene and used according to the manufacturers' instructions.

3. DNA Sequencing

Sequence analysis of DNA molecules was carried out according to the dideoxy chain termination method of Sanger et al. The primers used for sequencing the sbsA gene were constructed on the basis of the already published sbsA sequence (Kuen et al., Gene 145 (1994), 115-120).

4. PCR Amplification of sbsA

PCR amplification of the sbsA gene was carried out according to example 4 of PCT/EP98/04723.

The PCR-amplified products were electrophoretically fractionated on a 0.8% agarose gel and purified for cloning using the Gene Clean system (BIO101 La Jolla, Calif., USA).

5. Cloning of the SbsA Gene

5.1 Cytoplasmic Expression Vector

The sbsA gene, obtained by PCR and 3.79 kb in length, was purified and cleaved with restriction endonucleases XbaI and BamHI. The resulting XbaI-BamHI fragment was cloned into the corresponding restriction sites of vector pPLcAT10 so that the sbsA gene was under transcriptional control of the pL promoter located upstream. The ATG start codon of the sbsA sequence was reconstructed by the cloning procedure. The cloned sbsA sequence contained the N-terminal sbsA signal sequence and ended 20 nt after the transcription terminator. The resulting vector was denoted pBK4.

5.2 Periplasmic Expression Vector

The sbsA gene was cloned without signal sequence and with a stop codon at the 3′ end into the polylinker of the commercially available plasmid pMAL-P2 (New England Biolabs). The resulting pMAL-A plasmid contains a tac promoter-controlled fusion gene comprising the malE gene including the signal sequence thereof and also the sbsA gene without the signal sequence thereof. A factor Xa cleavage site is located between the two domains.

6. Recombinant Coexpression of the SbsA Gene in the cytoplasm and Periplasm of E.coli

E.coli K12 cells, cotransformed with pBK4 and pMAL-A, were cultured at 28° C. until reaching an optical density OD₆₀₀ of 0.3. Then cytoplasmic expression of sbsA was induced by increasing the culturing temperature from 28° C. to 42° C. Periplasmic expression of sbsA was induced by adding 1 mM of the lac inducer IPTG. 1.5 ml aliquots were removed before and 1, 2, 3 and 5 hours after induction of sbsA expression. E.coli pop2135/pPLcAT10 (cultured under the same conditions) and B.stearothermophilus PV72 were used as controls.

Culture supernatants and cell extracts from all samples were studied for expression of the S-layer protein by SDS-PAGE and Western immunoblotting.

For the Western blot, the proteins were transferred onto a nitrocellulose membrane and incubated with a polyclonal anti-SbsA antiserum from rabbits. Preparation of this antiserum is described in Egelseer et al. (J Bacteriol.177 (1995), 1444-1451). Bound SbsA-specific antibodies were detected using a conjugate of goat anti-rabbit IgG and alkaline phosphatase.

In cytoplasmic extracts of the cotransformed E.coli cells an additional strong protein band having about the same molecular weight as the wild type SbsA protein was found.

Analysis of the crude extract of E.coli DH5α cells (Hanahan (1983) supra) transformed with PMAL-A showed expression of a MalE-SbsA fusion polypeptide having a molecular weight of approx. 170 kDa in the periplasmic fraction of the cell extract, which was produced by a cold osmotic shock.procedure (Neu and Heppel, J. Biol. Chem. 240 (1965); 3685-3692).

7. Coexpression of the SbsB )Protein in the Cytoplasm and Periplasm

As described in examples 5 and 6, the sbsB gene was cloned into plasmids pMAL-P2 and pPLcAT10, resulting in plasmids pMAL-B and pBK6.

It was possible to detect the presence of the SbsB protein in the cytoplasm and periplasm of E.coli cells transformed with plasmids pMAL-B and pBK6.

8. Immobilized PHB Synthase in the Cytoplasmic Membrane of E.coli

Polyhydroxyalkanoates (PHA) are bacterial storage substances which are formed in a natural producer when phosphorus, sulfur or oxygen are limited but a carbon source is sufficiently present. They consist of esterified monomers of hydroxy fatty acids and form water-insoluble polymers which are distinguished depending on the position of the hydroxyl group and the length of the side chains. The most prominent PHA is poly(R)-3-hydroxybutyrate (P(3-HB)), an unbranched homopolymer of (R)-3-hydroxybutyric acid P(3-HB)).

In the Gram-negative, facultative chemolithotrophic oxyhydrogen bacterium Ralstonia eutropha the genes responsible for PHB systhesis, phbA, phbB and phbc, are organized in one operon (phbCAB) (Schubert et al., J. Bacteriol (1998), 170:5837). The nucleotide sequences of the open reading frames and also of the translation regions of said genes have been published (Steinbuchel, A. Polyhydroxy alcanoic acids, in: Biomaterials (1991), 123-213).

Within the study of the structure/function relation of PHB synthase, various insertion mutants and deletion mutants and also fusion proteins were prepared and changes in the enzyme activity were determined (Kalousek, S. PhD thesis, University of Vienna (1993)). From this work, plasmid pPHB-L originates which contains a gene which codes for a fusion protein composed of P(3-HB) synthase (588 of 590 amino acids) and a membrane anchor from the C-terminal sequence of the lysis protein of phage MS2. Cells growing on solid medium+1% glucose accumulate up to 60% (w/w) P-(3-HB) granules when expressing pPHB-L.

The membrane-anchored PHB synthase thus is enzymatically fully functional.

9. Recombinant Expression of (2,5-diketo-D-gluconic Acid) Reductase From a Plasmid in Bacteria; and Immobilization Thereof to Bacterial S-layers

Expression of a recombinant plasmid in a bacterial strain should enable said strain to produce 2-KLG directly from D-glucose in a single step (single fermentation). For this purpose, an enzyme required for the reduction to 2-KLG (2,5-DKG reductase from Corynebacterium sp. ATTC. 31090) was cloned into a strain producing 2,5-diketo-D-gluconic acid (2,5-DKG).

Using the vector pSL coding for a surface layer gene (sbsA) increased the stability of 2,5-DKG reductase. In this connection the S-layer protein (SbsA)-served as a matrix for 2,5-DKG reductase. By inserting 2,5-DKG reductase at 4 different sites within the sbsA gene, a recombinant protein having the ability to form self-assembly products was found.

To this end, sbsA-2,5 dkg reductase fusion genes were prepared which-carry the 2,5-dkg gene at.four different positions of the sbsA gene (positions 581, 881, 916 and 2649). E.coli pop2135 served as host cell. Correct cloning was checked by sequence analyses of the inserted gene and the neighboring regions. It was possible by SDS-PAGE and Western blot analyses to show stable expression of the fusion proteins. After successful expression in E.coli, the plasmids were transformed into Pectobacterium cypripedii HaPO1.

It was possible by means of SDS-PAGE and Western blot to detect in P.cypripedii HaPO1, too, stable expression of the SbsA-2,5 DKG reductase fusion protein.

10. Other Enzymes Immobilized to S-layers

The enzyme luciferase (genes luxA and luxB) and green fluorescent protein (gfp) were also fused to the sbsA gene, in order to generate in this way light and fluorescence, respectively.

4 1 3687 DNA Bacillus stearothermophilus CDS (1)..(3684) 1 atg gat agg aaa aaa gct gtg aaa cta gca aca gca agt gct att gca 48 Met Asp Arg Lys Lys Ala Val Lys Leu Ala Thr Ala Ser Ala Ile Ala -30 -25 -20 -15 gca agt gca ttt gtc gct gca aat cca aac gct tct gaa gcg gct aca 96 Ala Ser Ala Phe Val Ala Ala Asn Pro Asn Ala Ser Glu Ala Ala Thr -10 -5 -1 1 gat gta gca aca gta gta agc caa gca aaa gca cag ttc aaa aaa gca 144 Asp Val Ala Thr Val Val Ser Gln Ala Lys Ala Gln Phe Lys Lys Ala 5 10 15 tac tat act tac agc cat aca gta acg gaa act ggt gaa ttc cca aac 192 Tyr Tyr Thr Tyr Ser His Thr Val Thr Glu Thr Gly Glu Phe Pro Asn 20 25 30 att aac gat gta tat gct gaa tac aac aaa gcg aaa aaa cga tac cgt 240 Ile Asn Asp Val Tyr Ala Glu Tyr Asn Lys Ala Lys Lys Arg Tyr Arg 35 40 45 50 gat gcg gta gca tta gtg aat aaa gca ggt ggc gcg aaa aaa gac gct 288 Asp Ala Val Ala Leu Val Asn Lys Ala Gly Gly Ala Lys Lys Asp Ala 55 60 65 tac tta gct gat tta caa aaa gaa tat gaa act tac gtt ttc aaa gca 336 Tyr Leu Ala Asp Leu Gln Lys Glu Tyr Glu Thr Tyr Val Phe Lys Ala 70 75 80 aac cct aaa tct ggc gaa gct cgt gta gca act tac atc gat gct tac 384 Asn Pro Lys Ser Gly Glu Ala Arg Val Ala Thr Tyr Ile Asp Ala Tyr 85 90 95 aac tat gca aca aaa tta gac gaa atg cgc caa gag cta gag gct gct 432 Asn Tyr Ala Thr Lys Leu Asp Glu Met Arg Gln Glu Leu Glu Ala Ala 100 105 110 gtt caa gca aaa gat tta gaa aaa gca gaa caa tac tat cac aaa att 480 Val Gln Ala Lys Asp Leu Glu Lys Ala Glu Gln Tyr Tyr His Lys Ile 115 120 125 130 cct tat gaa att aaa act cgc aca gtc att tta gat cgc gta tat ggt 528 Pro Tyr Glu Ile Lys Thr Arg Thr Val Ile Leu Asp Arg Val Tyr Gly 135 140 145 aaa aca act cgt gat tta ctt cgc tct aca ttt aaa gca aaa gca caa 576 Lys Thr Thr Arg Asp Leu Leu Arg Ser Thr Phe Lys Ala Lys Ala Gln 150 155 160 gaa ctt cgc gac agc tta att tat gat att acc gtt gca atg aaa gcg 624 Glu Leu Arg Asp Ser Leu Ile Tyr Asp Ile Thr Val Ala Met Lys Ala 165 170 175 cgc gaa gta caa gac gct gtg aaa gca ggc aat tta gac aaa gct aaa 672 Arg Glu Val Gln Asp Ala Val Lys Ala Gly Asn Leu Asp Lys Ala Lys 180 185 190 gct gct gtt gat caa atc aat caa tac tta cca aaa gta aca gat gct 720 Ala Ala Val Asp Gln Ile Asn Gln Tyr Leu Pro Lys Val Thr Asp Ala 195 200 205 210 ttc aaa act gaa cta aca gaa gta gcg aaa aaa gca tta gat gca gat 768 Phe Lys Thr Glu Leu Thr Glu Val Ala Lys Lys Ala Leu Asp Ala Asp 215 220 225 gaa gct gcg ctt act cca aaa gtt gaa agt gta agt gcg att aac act 816 Glu Ala Ala Leu Thr Pro Lys Val Glu Ser Val Ser Ala Ile Asn Thr 230 235 240 caa aac aaa gct gtt gaa tta aca gca gta cca gtg aac gga aca cta 864 Gln Asn Lys Ala Val Glu Leu Thr Ala Val Pro Val Asn Gly Thr Leu 245 250 255 aaa tta caa ctt tca gct gct gca aat gaa gat aca gta aac gta aat 912 Lys Leu Gln Leu Ser Ala Ala Ala Asn Glu Asp Thr Val Asn Val Asn 260 265 270 act gta cgt atc tat aaa gtg gac ggt aac att cca ttt gcc ctt aat 960 Thr Val Arg Ile Tyr Lys Val Asp Gly Asn Ile Pro Phe Ala Leu Asn 275 280 285 290 acg gca gat gtt tct tta tct aca gac gga aaa act atc act gtg gat 1008 Thr Ala Asp Val Ser Leu Ser Thr Asp Gly Lys Thr Ile Thr Val Asp 295 300 305 gct tca act cca ttc gaa aat aat acg gag tat aaa gta gta gtt aaa 1056 Ala Ser Thr Pro Phe Glu Asn Asn Thr Glu Tyr Lys Val Val Val Lys 310 315 320 ggt att aaa gac aaa aat ggc aaa gaa ttt aaa gaa gat gca ttc act 1104 Gly Ile Lys Asp Lys Asn Gly Lys Glu Phe Lys Glu Asp Ala Phe Thr 325 330 335 ttc aag ctt cga aat gat gct gta gtt act caa gtg ttt gga act aat 1152 Phe Lys Leu Arg Asn Asp Ala Val Val Thr Gln Val Phe Gly Thr Asn 340 345 350 gta aca aac aac act tct gta aac tta gca gca ggt act ttc gac act 1200 Val Thr Asn Asn Thr Ser Val Asn Leu Ala Ala Gly Thr Phe Asp Thr 355 360 365 370 gac gat act tta aca gta gta ttt gat aag ttg tta gca cct gaa act 1248 Asp Asp Thr Leu Thr Val Val Phe Asp Lys Leu Leu Ala Pro Glu Thr 375 380 385 gta aac agc tcg aac gtt act att aca gat gtt gaa act gga aaa cgc 1296 Val Asn Ser Ser Asn Val Thr Ile Thr Asp Val Glu Thr Gly Lys Arg 390 395 400 att cca gta att gca tct act tct ggt tct aca att act att acg tta 1344 Ile Pro Val Ile Ala Ser Thr Ser Gly Ser Thr Ile Thr Ile Thr Leu 405 410 415 aaa gaa gcg tta gta act ggt aaa caa tat aaa ctt gct atc aat aat 1392 Lys Glu Ala Leu Val Thr Gly Lys Gln Tyr Lys Leu Ala Ile Asn Asn 420 425 430 gtt aaa aca tta act ggt tac aat gca gaa gct tac gag tta gtg ttc 1440 Val Lys Thr Leu Thr Gly Tyr Asn Ala Glu Ala Tyr Glu Leu Val Phe 435 440 445 450 act gca aac gca tca gca cca act gtt gct acc gct cct act act tta 1488 Thr Ala Asn Ala Ser Ala Pro Thr Val Ala Thr Ala Pro Thr Thr Leu 455 460 465 ggt ggt aca act tta tct act ggt tct ctt aca aca aat gtt tgg ggt 1536 Gly Gly Thr Thr Leu Ser Thr Gly Ser Leu Thr Thr Asn Val Trp Gly 470 475 480 aaa ttg gct ggt ggt gtg aat gaa gct gga act tat tat cct ggt ctt 1584 Lys Leu Ala Gly Gly Val Asn Glu Ala Gly Thr Tyr Tyr Pro Gly Leu 485 490 495 caa ttc aca aca acg ttt gct act aag tta gac gaa tct act tta gct 1632 Gln Phe Thr Thr Thr Phe Ala Thr Lys Leu Asp Glu Ser Thr Leu Ala 500 505 510 gat aac ttt gta tta gtt gaa aaa gaa tct ggt aca gtt gtt gct tct 1680 Asp Asn Phe Val Leu Val Glu Lys Glu Ser Gly Thr Val Val Ala Ser 515 520 525 530 gaa cta aaa tat aat gca gac gct aaa atg gta act tta gtg cca aaa 1728 Glu Leu Lys Tyr Asn Ala Asp Ala Lys Met Val Thr Leu Val Pro Lys 535 540 545 gcg gac ctt aaa gaa aat aca atc tat caa atc aaa att aaa aaa ggc 1776 Ala Asp Leu Lys Glu Asn Thr Ile Tyr Gln Ile Lys Ile Lys Lys Gly 550 555 560 ttg aag tcc gat aaa ggt att gaa tta ggc act gtt aac gag aaa aca 1824 Leu Lys Ser Asp Lys Gly Ile Glu Leu Gly Thr Val Asn Glu Lys Thr 565 570 575 tat gag ttc aaa act caa gac tta act gct cct aca gtt att agc gta 1872 Tyr Glu Phe Lys Thr Gln Asp Leu Thr Ala Pro Thr Val Ile Ser Val 580 585 590 acg tct aaa aat ggc gac gct gga tta aaa gta act gaa gct caa gaa 1920 Thr Ser Lys Asn Gly Asp Ala Gly Leu Lys Val Thr Glu Ala Gln Glu 595 600 605 610 ttt act gtg aag ttc tca gag aat tta aat aca ttt aat gct aca acc 1968 Phe Thr Val Lys Phe Ser Glu Asn Leu Asn Thr Phe Asn Ala Thr Thr 615 620 625 gtt tcg ggt agc aca atc aca tac ggt caa gtt gct gta gta aaa gcg 2016 Val Ser Gly Ser Thr Ile Thr Tyr Gly Gln Val Ala Val Val Lys Ala 630 635 640 ggt gca aac tta tct gct ctt aca gca agt gac atc att cca gct agt 2064 Gly Ala Asn Leu Ser Ala Leu Thr Ala Ser Asp Ile Ile Pro Ala Ser 645 650 655 gtt gaa gcg gtt act ggt caa gat gga aca tac aaa gtg aaa gtt gct 2112 Val Glu Ala Val Thr Gly Gln Asp Gly Thr Tyr Lys Val Lys Val Ala 660 665 670 gct aac caa tta gaa cgt aac caa ggg tac aaa tta gta gtg ttc ggt 2160 Ala Asn Gln Leu Glu Arg Asn Gln Gly Tyr Lys Leu Val Val Phe Gly 675 680 685 690 aaa ggt gca aca gct cct gtt aaa gat gct gca aat gca aat act tta 2208 Lys Gly Ala Thr Ala Pro Val Lys Asp Ala Ala Asn Ala Asn Thr Leu 695 700 705 gca act aac tat atc tat aca ttt aca act gaa ggt caa gac gta aca 2256 Ala Thr Asn Tyr Ile Tyr Thr Phe Thr Thr Glu Gly Gln Asp Val Thr 710 715 720 gca cca acg gtt aca aaa gta ttc aaa ggt gat tct tta aaa gac gct 2304 Ala Pro Thr Val Thr Lys Val Phe Lys Gly Asp Ser Leu Lys Asp Ala 725 730 735 gat gca gtt act aca ctt acg aac gtt gat gca ggt caa aaa ttc act 2352 Asp Ala Val Thr Thr Leu Thr Asn Val Asp Ala Gly Gln Lys Phe Thr 740 745 750 atc caa ttt agc gaa gaa tta aaa act tct agt ggt tct tta gtg ggt 2400 Ile Gln Phe Ser Glu Glu Leu Lys Thr Ser Ser Gly Ser Leu Val Gly 755 760 765 770 ggc aaa gta act gtc gag aaa tta aca aac aac gga tgg gta gat gct 2448 Gly Lys Val Thr Val Glu Lys Leu Thr Asn Asn Gly Trp Val Asp Ala 775 780 785 ggt act gga aca act gta tca gtt gct cct aag aca gat gca aat ggt 2496 Gly Thr Gly Thr Thr Val Ser Val Ala Pro Lys Thr Asp Ala Asn Gly 790 795 800 aaa gta aca gct gct gtg gtt aca tta act ggt ctt gac aat aac gac 2544 Lys Val Thr Ala Ala Val Val Thr Leu Thr Gly Leu Asp Asn Asn Asp 805 810 815 aaa gat gcg aaa ttg cgt ctg gta gta gat aag tct tct act gat gga 2592 Lys Asp Ala Lys Leu Arg Leu Val Val Asp Lys Ser Ser Thr Asp Gly 820 825 830 att gct gat gta gct ggt aat gta att aag gaa aaa gat att tta att 2640 Ile Ala Asp Val Ala Gly Asn Val Ile Lys Glu Lys Asp Ile Leu Ile 835 840 845 850 cgt tac aac agc tgg aga cac act gta gct tct gtg aaa gct gct gct 2688 Arg Tyr Asn Ser Trp Arg His Thr Val Ala Ser Val Lys Ala Ala Ala 855 860 865 gac aaa gat ggt caa aac gct tct gct gca ttc cca aca agc act gca 2736 Asp Lys Asp Gly Gln Asn Ala Ser Ala Ala Phe Pro Thr Ser Thr Ala 870 875 880 att gat aca act aag agc tta tta gtt gaa ttc aat gaa act gat tta 2784 Ile Asp Thr Thr Lys Ser Leu Leu Val Glu Phe Asn Glu Thr Asp Leu 885 890 895 gcg gaa gtt aaa cct gag aac atc gtt gtt aaa gat gca gca ggt aat 2832 Ala Glu Val Lys Pro Glu Asn Ile Val Val Lys Asp Ala Ala Gly Asn 900 905 910 gcg gta gct ggt act gta aca gca tta gac ggt tct aca aat aaa ttt 2880 Ala Val Ala Gly Thr Val Thr Ala Leu Asp Gly Ser Thr Asn Lys Phe 915 920 925 930 gta ttc act cca tct caa gaa tta aaa gct ggt aca gtt tac tct gta 2928 Val Phe Thr Pro Ser Gln Glu Leu Lys Ala Gly Thr Val Tyr Ser Val 935 940 945 aca att gac ggt gtg aga gat aaa gta ggt aac aca atc tct aaa tac 2976 Thr Ile Asp Gly Val Arg Asp Lys Val Gly Asn Thr Ile Ser Lys Tyr 950 955 960 att act tcg ttc aag act gta tct gcg aat cca acg tta tct tca atc 3024 Ile Thr Ser Phe Lys Thr Val Ser Ala Asn Pro Thr Leu Ser Ser Ile 965 970 975 agc att gct gac ggt gca gtt aac gtt gac cgt tct aaa aca att aca 3072 Ser Ile Ala Asp Gly Ala Val Asn Val Asp Arg Ser Lys Thr Ile Thr 980 985 990 att gaa ttc agc gat tca gtt cca aac cca aca atc act ctt aag 3117 Ile Glu Phe Ser Asp Ser Val Pro Asn Pro Thr Ile Thr Leu Lys 995 1000 1005 aag gct gac gga act tca ttt act aat tac act tta gta aat gta 3162 Lys Ala Asp Gly Thr Ser Phe Thr Asn Tyr Thr Leu Val Asn Val 1010 1015 1020 aat aat gaa aat aaa aca tac aaa att gta ttc cac aaa ggt gta 3207 Asn Asn Glu Asn Lys Thr Tyr Lys Ile Val Phe His Lys Gly Val 1025 1030 1035 aca ctt gac gag ttt act caa tat gag tta gca gtt tca aaa gat 3252 Thr Leu Asp Glu Phe Thr Gln Tyr Glu Leu Ala Val Ser Lys Asp 1040 1045 1050 ttt caa act ggt act gat att gat agc aaa gtt aca ttc atc aca 3297 Phe Gln Thr Gly Thr Asp Ile Asp Ser Lys Val Thr Phe Ile Thr 1055 1060 1065 ggt tct gtt gct act gac gaa gta aaa cct gct cta gta ggc gtt 3342 Gly Ser Val Ala Thr Asp Glu Val Lys Pro Ala Leu Val Gly Val 1070 1075 1080 ggt tca tgg aat gga aca agc tat act cag gat gct gca gca aca 3387 Gly Ser Trp Asn Gly Thr Ser Tyr Thr Gln Asp Ala Ala Ala Thr 1085 1090 1095 cga ctt cgg tct gta gct gac ttc gtt gcg gag cca gtt gcc ctt 3432 Arg Leu Arg Ser Val Ala Asp Phe Val Ala Glu Pro Val Ala Leu 1100 1105 1110 caa ttc tca gaa ggt atc gat tta acg aat gca act gtg aca gta 3477 Gln Phe Ser Glu Gly Ile Asp Leu Thr Asn Ala Thr Val Thr Val 1115 1120 1125 aca aat att act gat gat aaa act gtt gaa gtt att tca aaa gag 3522 Thr Asn Ile Thr Asp Asp Lys Thr Val Glu Val Ile Ser Lys Glu 1130 1135 1140 agt gta gac gca gac cat gat gca ggt gct act aag gag aca tta 3567 Ser Val Asp Ala Asp His Asp Ala Gly Ala Thr Lys Glu Thr Leu 1145 1150 1155 gta att aac aca gtt act cct tta gta ctt gat aac agc aag act 3612 Val Ile Asn Thr Val Thr Pro Leu Val Leu Asp Asn Ser Lys Thr 1160 1165 1170 tat aag att gtt gta agt gga gtt aaa gat gca gca ggt aat gtt 3657 Tyr Lys Ile Val Val Ser Gly Val Lys Asp Ala Ala Gly Asn Val 1175 1180 1185 gca gat act att aca ttc tat att aag taa 3687 Ala Asp Thr Ile Thr Phe Tyr Ile Lys 1190 1195 2 1228 PRT Bacillus stearothermophilus 2 Met Asp Arg Lys Lys Ala Val Lys Leu Ala Thr Ala Ser Ala Ile Ala -30 -25 -20 -15 Ala Ser Ala Phe Val Ala Ala Asn Pro Asn Ala Ser Glu Ala Ala Thr -10 -5 -1 1 Asp Val Ala Thr Val Val Ser Gln Ala Lys Ala Gln Phe Lys Lys Ala 5 10 15 Tyr Tyr Thr Tyr Ser His Thr Val Thr Glu Thr Gly Glu Phe Pro Asn 20 25 30 Ile Asn Asp Val Tyr Ala Glu Tyr Asn Lys Ala Lys Lys Arg Tyr Arg 35 40 45 50 Asp Ala Val Ala Leu Val Asn Lys Ala Gly Gly Ala Lys Lys Asp Ala 55 60 65 Tyr Leu Ala Asp Leu Gln Lys Glu Tyr Glu Thr Tyr Val Phe Lys Ala 70 75 80 Asn Pro Lys Ser Gly Glu Ala Arg Val Ala Thr Tyr Ile Asp Ala Tyr 85 90 95 Asn Tyr Ala Thr Lys Leu Asp Glu Met Arg Gln Glu Leu Glu Ala Ala 100 105 110 Val Gln Ala Lys Asp Leu Glu Lys Ala Glu Gln Tyr Tyr His Lys Ile 115 120 125 130 Pro Tyr Glu Ile Lys Thr Arg Thr Val Ile Leu Asp Arg Val Tyr Gly 135 140 145 Lys Thr Thr Arg Asp Leu Leu Arg Ser Thr Phe Lys Ala Lys Ala Gln 150 155 160 Glu Leu Arg Asp Ser Leu Ile Tyr Asp Ile Thr Val Ala Met Lys Ala 165 170 175 Arg Glu Val Gln Asp Ala Val Lys Ala Gly Asn Leu Asp Lys Ala Lys 180 185 190 Ala Ala Val Asp Gln Ile Asn Gln Tyr Leu Pro Lys Val Thr Asp Ala 195 200 205 210 Phe Lys Thr Glu Leu Thr Glu Val Ala Lys Lys Ala Leu Asp Ala Asp 215 220 225 Glu Ala Ala Leu Thr Pro Lys Val Glu Ser Val Ser Ala Ile Asn Thr 230 235 240 Gln Asn Lys Ala Val Glu Leu Thr Ala Val Pro Val Asn Gly Thr Leu 245 250 255 Lys Leu Gln Leu Ser Ala Ala Ala Asn Glu Asp Thr Val Asn Val Asn 260 265 270 Thr Val Arg Ile Tyr Lys Val Asp Gly Asn Ile Pro Phe Ala Leu Asn 275 280 285 290 Thr Ala Asp Val Ser Leu Ser Thr Asp Gly Lys Thr Ile Thr Val Asp 295 300 305 Ala Ser Thr Pro Phe Glu Asn Asn Thr Glu Tyr Lys Val Val Val Lys 310 315 320 Gly Ile Lys Asp Lys Asn Gly Lys Glu Phe Lys Glu Asp Ala Phe Thr 325 330 335 Phe Lys Leu Arg Asn Asp Ala Val Val Thr Gln Val Phe Gly Thr Asn 340 345 350 Val Thr Asn Asn Thr Ser Val Asn Leu Ala Ala Gly Thr Phe Asp Thr 355 360 365 370 Asp Asp Thr Leu Thr Val Val Phe Asp Lys Leu Leu Ala Pro Glu Thr 375 380 385 Val Asn Ser Ser Asn Val Thr Ile Thr Asp Val Glu Thr Gly Lys Arg 390 395 400 Ile Pro Val Ile Ala Ser Thr Ser Gly Ser Thr Ile Thr Ile Thr Leu 405 410 415 Lys Glu Ala Leu Val Thr Gly Lys Gln Tyr Lys Leu Ala Ile Asn Asn 420 425 430 Val Lys Thr Leu Thr Gly Tyr Asn Ala Glu Ala Tyr Glu Leu Val Phe 435 440 445 450 Thr Ala Asn Ala Ser Ala Pro Thr Val Ala Thr Ala Pro Thr Thr Leu 455 460 465 Gly Gly Thr Thr Leu Ser Thr Gly Ser Leu Thr Thr Asn Val Trp Gly 470 475 480 Lys Leu Ala Gly Gly Val Asn Glu Ala Gly Thr Tyr Tyr Pro Gly Leu 485 490 495 Gln Phe Thr Thr Thr Phe Ala Thr Lys Leu Asp Glu Ser Thr Leu Ala 500 505 510 Asp Asn Phe Val Leu Val Glu Lys Glu Ser Gly Thr Val Val Ala Ser 515 520 525 530 Glu Leu Lys Tyr Asn Ala Asp Ala Lys Met Val Thr Leu Val Pro Lys 535 540 545 Ala Asp Leu Lys Glu Asn Thr Ile Tyr Gln Ile Lys Ile Lys Lys Gly 550 555 560 Leu Lys Ser Asp Lys Gly Ile Glu Leu Gly Thr Val Asn Glu Lys Thr 565 570 575 Tyr Glu Phe Lys Thr Gln Asp Leu Thr Ala Pro Thr Val Ile Ser Val 580 585 590 Thr Ser Lys Asn Gly Asp Ala Gly Leu Lys Val Thr Glu Ala Gln Glu 595 600 605 610 Phe Thr Val Lys Phe Ser Glu Asn Leu Asn Thr Phe Asn Ala Thr Thr 615 620 625 Val Ser Gly Ser Thr Ile Thr Tyr Gly Gln Val Ala Val Val Lys Ala 630 635 640 Gly Ala Asn Leu Ser Ala Leu Thr Ala Ser Asp Ile Ile Pro Ala Ser 645 650 655 Val Glu Ala Val Thr Gly Gln Asp Gly Thr Tyr Lys Val Lys Val Ala 660 665 670 Ala Asn Gln Leu Glu Arg Asn Gln Gly Tyr Lys Leu Val Val Phe Gly 675 680 685 690 Lys Gly Ala Thr Ala Pro Val Lys Asp Ala Ala Asn Ala Asn Thr Leu 695 700 705 Ala Thr Asn Tyr Ile Tyr Thr Phe Thr Thr Glu Gly Gln Asp Val Thr 710 715 720 Ala Pro Thr Val Thr Lys Val Phe Lys Gly Asp Ser Leu Lys Asp Ala 725 730 735 Asp Ala Val Thr Thr Leu Thr Asn Val Asp Ala Gly Gln Lys Phe Thr 740 745 750 Ile Gln Phe Ser Glu Glu Leu Lys Thr Ser Ser Gly Ser Leu Val Gly 755 760 765 770 Gly Lys Val Thr Val Glu Lys Leu Thr Asn Asn Gly Trp Val Asp Ala 775 780 785 Gly Thr Gly Thr Thr Val Ser Val Ala Pro Lys Thr Asp Ala Asn Gly 790 795 800 Lys Val Thr Ala Ala Val Val Thr Leu Thr Gly Leu Asp Asn Asn Asp 805 810 815 Lys Asp Ala Lys Leu Arg Leu Val Val Asp Lys Ser Ser Thr Asp Gly 820 825 830 Ile Ala Asp Val Ala Gly Asn Val Ile Lys Glu Lys Asp Ile Leu Ile 835 840 845 850 Arg Tyr Asn Ser Trp Arg His Thr Val Ala Ser Val Lys Ala Ala Ala 855 860 865 Asp Lys Asp Gly Gln Asn Ala Ser Ala Ala Phe Pro Thr Ser Thr Ala 870 875 880 Ile Asp Thr Thr Lys Ser Leu Leu Val Glu Phe Asn Glu Thr Asp Leu 885 890 895 Ala Glu Val Lys Pro Glu Asn Ile Val Val Lys Asp Ala Ala Gly Asn 900 905 910 Ala Val Ala Gly Thr Val Thr Ala Leu Asp Gly Ser Thr Asn Lys Phe 915 920 925 930 Val Phe Thr Pro Ser Gln Glu Leu Lys Ala Gly Thr Val Tyr Ser Val 935 940 945 Thr Ile Asp Gly Val Arg Asp Lys Val Gly Asn Thr Ile Ser Lys Tyr 950 955 960 Ile Thr Ser Phe Lys Thr Val Ser Ala Asn Pro Thr Leu Ser Ser Ile 965 970 975 Ser Ile Ala Asp Gly Ala Val Asn Val Asp Arg Ser Lys Thr Ile Thr 980 985 990 Ile Glu Phe Ser Asp Ser Val Pro Asn Pro Thr Ile Thr Leu Lys 995 1000 1005 Lys Ala Asp Gly Thr Ser Phe Thr Asn Tyr Thr Leu Val Asn Val 1010 1015 1020 Asn Asn Glu Asn Lys Thr Tyr Lys Ile Val Phe His Lys Gly Val 1025 1030 1035 Thr Leu Asp Glu Phe Thr Gln Tyr Glu Leu Ala Val Ser Lys Asp 1040 1045 1050 Phe Gln Thr Gly Thr Asp Ile Asp Ser Lys Val Thr Phe Ile Thr 1055 1060 1065 Gly Ser Val Ala Thr Asp Glu Val Lys Pro Ala Leu Val Gly Val 1070 1075 1080 Gly Ser Trp Asn Gly Thr Ser Tyr Thr Gln Asp Ala Ala Ala Thr 1085 1090 1095 Arg Leu Arg Ser Val Ala Asp Phe Val Ala Glu Pro Val Ala Leu 1100 1105 1110 Gln Phe Ser Glu Gly Ile Asp Leu Thr Asn Ala Thr Val Thr Val 1115 1120 1125 Thr Asn Ile Thr Asp Asp Lys Thr Val Glu Val Ile Ser Lys Glu 1130 1135 1140 Ser Val Asp Ala Asp His Asp Ala Gly Ala Thr Lys Glu Thr Leu 1145 1150 1155 Val Ile Asn Thr Val Thr Pro Leu Val Leu Asp Asn Ser Lys Thr 1160 1165 1170 Tyr Lys Ile Val Val Ser Gly Val Lys Asp Ala Ala Gly Asn Val 1175 1180 1185 Ala Asp Thr Ile Thr Phe Tyr Ile Lys 1190 1195 3 2766 DNA Bacillus stearothermophilus CDS (1)..(2763) 3 atg gct tat caa cct aag tcc tat cgc aag ttt gtt gcg aca act gca 48 Met Ala Tyr Gln Pro Lys Ser Tyr Arg Lys Phe Val Ala Thr Thr Ala -30 -25 -20 aca gct gcc atg gta gca tct gcg gta gct cct gta gta tct gca gca 96 Thr Ala Ala Met Val Ala Ser Ala Val Ala Pro Val Val Ser Ala Ala -15 -10 -5 -1 1 agc ttc aca gat gtt gcg ccg caa tat aaa gat gcg atc gat ttc tta 144 Ser Phe Thr Asp Val Ala Pro Gln Tyr Lys Asp Ala Ile Asp Phe Leu 5 10 15 gta tca act ggt gca aca aaa ggt aaa aca gaa aca aaa ttc ggc gtt 192 Val Ser Thr Gly Ala Thr Lys Gly Lys Thr Glu Thr Lys Phe Gly Val 20 25 30 tac gat gaa atc act cgt cta gat gcg gca gtt att ctt gca aga gta 240 Tyr Asp Glu Ile Thr Arg Leu Asp Ala Ala Val Ile Leu Ala Arg Val 35 40 45 tta aaa cta gac gtt gac aac gca aaa gac gca ggc ttc aca gat gtg 288 Leu Lys Leu Asp Val Asp Asn Ala Lys Asp Ala Gly Phe Thr Asp Val 50 55 60 65 cca aaa gac cgt gca aaa tac gtc aac gcg ctt gta gaa gct ggc gta 336 Pro Lys Asp Arg Ala Lys Tyr Val Asn Ala Leu Val Glu Ala Gly Val 70 75 80 tta aac ggt aaa gca cct ggc aaa ttt ggt gca tac gac cca tta act 384 Leu Asn Gly Lys Ala Pro Gly Lys Phe Gly Ala Tyr Asp Pro Leu Thr 85 90 95 cgc gtt gaa atg gca aaa atc atc gcg aac cgt tac aaa tta aaa gct 432 Arg Val Glu Met Ala Lys Ile Ile Ala Asn Arg Tyr Lys Leu Lys Ala 100 105 110 gac gat gta aaa ctt cca ttc act gat gta aac gat aca tgg gca cca 480 Asp Asp Val Lys Leu Pro Phe Thr Asp Val Asn Asp Thr Trp Ala Pro 115 120 125 tac gta aaa gcg ctt tat aaa tac gaa gta acc aaa agg tta aaa cac 528 Tyr Val Lys Ala Leu Tyr Lys Tyr Glu Val Thr Lys Arg Leu Lys His 130 135 140 145 caa caa gct tcg gtg cat acc aaa aac atc act ctg cgt gac ttt gcg 576 Gln Gln Ala Ser Val His Thr Lys Asn Ile Thr Leu Arg Asp Phe Ala 150 155 160 caa ttt gta tat aga gcg gtg aat att aat gca gtg cca gaa ata gtt 624 Gln Phe Val Tyr Arg Ala Val Asn Ile Asn Ala Val Pro Glu Ile Val 165 170 175 gaa gta act gcg gtt aat tcg act aca gtg aaa gta aca ttc aat acg 672 Glu Val Thr Ala Val Asn Ser Thr Thr Val Lys Val Thr Phe Asn Thr 180 185 190 caa att gct gat gtt gat ttc aca aat ttt gct atc gat aac ggt tta 720 Gln Ile Ala Asp Val Asp Phe Thr Asn Phe Ala Ile Asp Asn Gly Leu 195 200 205 act gtt act aaa gca act ctt tct cgt gat aaa aaa tcc gta gag gtt 768 Thr Val Thr Lys Ala Thr Leu Ser Arg Asp Lys Lys Ser Val Glu Val 210 215 220 225 gtg gta aat aaa ccg ttt act cgt aat cag gaa tat aca att aca gcg 816 Val Val Asn Lys Pro Phe Thr Arg Asn Gln Glu Tyr Thr Ile Thr Ala 230 235 240 aca ggc att aaa aat tta aaa ggc gag acc gct aag gaa tta act ggt 864 Thr Gly Ile Lys Asn Leu Lys Gly Glu Thr Ala Lys Glu Leu Thr Gly 245 250 255 aag ttt gtt tgg tct gtt caa gat gcg gta act gtt gca cta aat aat 912 Lys Phe Val Trp Ser Val Gln Asp Ala Val Thr Val Ala Leu Asn Asn 260 265 270 agt tcg ctt aaa gtt gga gag gaa tct ggt tta act gta aaa gat cag 960 Ser Ser Leu Lys Val Gly Glu Glu Ser Gly Leu Thr Val Lys Asp Gln 275 280 285 gat ggc aaa gat gtt gta ggt gct aaa gta gaa ctt act tct tct aat 1008 Asp Gly Lys Asp Val Val Gly Ala Lys Val Glu Leu Thr Ser Ser Asn 290 295 300 305 act aat att gtt gta gtt tca agt ggc gaa gta tca gta tct gct gct 1056 Thr Asn Ile Val Val Val Ser Ser Gly Glu Val Ser Val Ser Ala Ala 310 315 320 aaa gtt aca gct gta aaa ccg gga aca gct gat gtt act gca aaa gtt 1104 Lys Val Thr Ala Val Lys Pro Gly Thr Ala Asp Val Thr Ala Lys Val 325 330 335 aca tta cca gat ggt gtt gta cta aca aat aca ttt aaa gtg aca gtt 1152 Thr Leu Pro Asp Gly Val Val Leu Thr Asn Thr Phe Lys Val Thr Val 340 345 350 aca gaa gtg cct gtg caa gta caa aat caa gga ttt act tta gtt gat 1200 Thr Glu Val Pro Val Gln Val Gln Asn Gln Gly Phe Thr Leu Val Asp 355 360 365 aat ctt tct aat gct cca cag aat aca gtt gca ttt aac aaa gct gag 1248 Asn Leu Ser Asn Ala Pro Gln Asn Thr Val Ala Phe Asn Lys Ala Glu 370 375 380 385 aaa gta act tca atg ttt gct gga gaa act aaa aca gtt gca atg tat 1296 Lys Val Thr Ser Met Phe Ala Gly Glu Thr Lys Thr Val Ala Met Tyr 390 395 400 gat act aaa aac ggt gat cct gaa act aaa cct gtt gat ttc aaa gat 1344 Asp Thr Lys Asn Gly Asp Pro Glu Thr Lys Pro Val Asp Phe Lys Asp 405 410 415 gca act gta cgt tca tta aat cca att att gca aca gct gct att aat 1392 Ala Thr Val Arg Ser Leu Asn Pro Ile Ile Ala Thr Ala Ala Ile Asn 420 425 430 ggt agt gag ctc ctt gtc aca gct aat gct ggc caa tct gga aaa gct 1440 Gly Ser Glu Leu Leu Val Thr Ala Asn Ala Gly Gln Ser Gly Lys Ala 435 440 445 tca ttt gaa gta aca ttt aaa gat aat aca aaa aga aca ttt aca gtt 1488 Ser Phe Glu Val Thr Phe Lys Asp Asn Thr Lys Arg Thr Phe Thr Val 450 455 460 465 gat gtg aaa aaa gac cct gta tta caa gat att aaa gta gat gca act 1536 Asp Val Lys Lys Asp Pro Val Leu Gln Asp Ile Lys Val Asp Ala Thr 470 475 480 tct gtt aaa ctt tcc gat gaa gct gtt ggc ggc ggg gaa gtt gaa gga 1584 Ser Val Lys Leu Ser Asp Glu Ala Val Gly Gly Gly Glu Val Glu Gly 485 490 495 gtt aac caa aaa acg att aaa gta agt gca gtt gac caa tac ggt aaa 1632 Val Asn Gln Lys Thr Ile Lys Val Ser Ala Val Asp Gln Tyr Gly Lys 500 505 510 gaa att aaa ttt ggt aca aaa ggt aaa gtt act gtt aca act aat aca 1680 Glu Ile Lys Phe Gly Thr Lys Gly Lys Val Thr Val Thr Thr Asn Thr 515 520 525 gaa gga cta gtt att aaa aat gta aat agc gat aat aca att gac ttt 1728 Glu Gly Leu Val Ile Lys Asn Val Asn Ser Asp Asn Thr Ile Asp Phe 530 535 540 545 gat agc ggc aat agt gca act gac caa ttt gtt gtc gtt gca aca aaa 1776 Asp Ser Gly Asn Ser Ala Thr Asp Gln Phe Val Val Val Ala Thr Lys 550 555 560 gac aaa att gtc aat ggt aaa gta gaa gtt aaa tat ttc aaa aat gct 1824 Asp Lys Ile Val Asn Gly Lys Val Glu Val Lys Tyr Phe Lys Asn Ala 565 570 575 agt gac aca aca cca act tca act aaa aca att act gtt aat gta gtg 1872 Ser Asp Thr Thr Pro Thr Ser Thr Lys Thr Ile Thr Val Asn Val Val 580 585 590 aat gta aaa gct gac gct aca cca gta gga tta gat att gta gca cct 1920 Asn Val Lys Ala Asp Ala Thr Pro Val Gly Leu Asp Ile Val Ala Pro 595 600 605 tct gaa att gat gtg aat gct cca aac act gct tct act gca gat gtt 1968 Ser Glu Ile Asp Val Asn Ala Pro Asn Thr Ala Ser Thr Ala Asp Val 610 615 620 625 gat ttt att aat ttc gaa agt gtt gag att tat aca ctc gat tct aat 2016 Asp Phe Ile Asn Phe Glu Ser Val Glu Ile Tyr Thr Leu Asp Ser Asn 630 635 640 ggt aac cgt ctt aaa aaa gtt act cca act gca act aca ctt gta ggt 2064 Gly Asn Arg Leu Lys Lys Val Thr Pro Thr Ala Thr Thr Leu Val Gly 645 650 655 act aat gat tat gtt gaa gtt aat ggg aat gta tta caa ttc aag ggt 2112 Thr Asn Asp Tyr Val Glu Val Asn Gly Asn Val Leu Gln Phe Lys Gly 660 665 670 aac gat gaa tta acg cta tta act tct tct agt aca gta aac gtt gat 2160 Asn Asp Glu Leu Thr Leu Leu Thr Ser Ser Ser Thr Val Asn Val Asp 675 680 685 gta aca gct gat gga att aca aaa cgt att cca gta aaa tat atc aac 2208 Val Thr Ala Asp Gly Ile Thr Lys Arg Ile Pro Val Lys Tyr Ile Asn 690 695 700 705 tct gca agt gta cct gcc agt gca aca gta gca aca agt cct gtt act 2256 Ser Ala Ser Val Pro Ala Ser Ala Thr Val Ala Thr Ser Pro Val Thr 710 715 720 gtt aag ctt aat tca agt gat aat gat tta aca ttt gaa gaa tta ata 2304 Val Lys Leu Asn Ser Ser Asp Asn Asp Leu Thr Phe Glu Glu Leu Ile 725 730 735 ttc ggt gta att gac cct aca caa tta gtc aaa gat gaa gac atc aac 2352 Phe Gly Val Ile Asp Pro Thr Gln Leu Val Lys Asp Glu Asp Ile Asn 740 745 750 gaa ttt att gca gtt tca aaa gcg gct aaa aat gat gga tat ttg tat 2400 Glu Phe Ile Ala Val Ser Lys Ala Ala Lys Asn Asp Gly Tyr Leu Tyr 755 760 765 aat aaa ccg ctt gta acg gtt aaa gat gca tca gga aaa gtt att cca 2448 Asn Lys Pro Leu Val Thr Val Lys Asp Ala Ser Gly Lys Val Ile Pro 770 775 780 785 aca ggt gca aat gtt tac ggt cta aat cat gat gca act aac gga aac 2496 Thr Gly Ala Asn Val Tyr Gly Leu Asn His Asp Ala Thr Asn Gly Asn 790 795 800 att tgg ttt gat gag gaa caa gct ggc tta gct aaa aaa ttt agt gat 2544 Ile Trp Phe Asp Glu Glu Gln Ala Gly Leu Ala Lys Lys Phe Ser Asp 805 810 815 gta cat ttt gat gtt gat ttt tca tta gct aac gtt gta aaa act ggt 2592 Val His Phe Asp Val Asp Phe Ser Leu Ala Asn Val Val Lys Thr Gly 820 825 830 agc ggt aca gtt tct tca tcg cca tca tta tct gac gca att caa ctt 2640 Ser Gly Thr Val Ser Ser Ser Pro Ser Leu Ser Asp Ala Ile Gln Leu 835 840 845 act aat tca ggc gat gca gta tcg ttt aca tta gtt atc aaa tca att 2688 Thr Asn Ser Gly Asp Ala Val Ser Phe Thr Leu Val Ile Lys Ser Ile 850 855 860 865 tat gtt aaa ggc gca gat aaa gat gat aat aac tta ctt gca gcc cct 2736 Tyr Val Lys Gly Ala Asp Lys Asp Asp Asn Asn Leu Leu Ala Ala Pro 870 875 880 gtt tct gtc aat gtg act gtg aca aaa taa 2766 Val Ser Val Asn Val Thr Val Thr Lys 885 890 4 921 PRT Bacillus stearothermophilus 4 Met Ala Tyr Gln Pro Lys Ser Tyr Arg Lys Phe Val Ala Thr Thr Ala 1 5 10 15 Thr Ala Ala Met Val Ala Ser Ala Val Ala Pro Val Val Ser Ala Ala 20 25 30 Ser Phe Thr Asp Val Ala Pro Gln Tyr Lys Asp Ala Ile Asp Phe Leu 35 40 45 Val Ser Thr Gly Ala Thr Lys Gly Lys Thr Glu Thr Lys Phe Gly Val 50 55 60 Tyr Asp Glu Ile Thr Arg Leu Asp Ala Ala Val Ile Leu Ala Arg Val 65 70 75 80 Leu Lys Leu Asp Val Asp Asn Ala Lys Asp Ala Gly Phe Thr Asp Val 85 90 95 Pro Lys Asp Arg Ala Lys Tyr Val Asn Ala Leu Val Glu Ala Gly Val 100 105 110 Leu Asn Gly Lys Ala Pro Gly Lys Phe Gly Ala Tyr Asp Pro Leu Thr 115 120 125 Arg Val Glu Met Ala Lys Ile Ile Ala Asn Arg Tyr Lys Leu Lys Ala 130 135 140 Asp Asp Val Lys Leu Pro Phe Thr Asp Val Asn Asp Thr Trp Ala Pro 145 150 155 160 Tyr Val Lys Ala Leu Tyr Lys Tyr Glu Val Thr Lys Arg Leu Lys His 165 170 175 Gln Gln Ala Ser Val His Thr Lys Asn Ile Thr Leu Arg Asp Phe Ala 180 185 190 Gln Phe Val Tyr Arg Ala Val Asn Ile Asn Ala Val Pro Glu Ile Val 195 200 205 Glu Val Thr Ala Val Asn Ser Thr Thr Val Lys Val Thr Phe Asn Thr 210 215 220 Gln Ile Ala Asp Val Asp Phe Thr Asn Phe Ala Ile Asp Asn Gly Leu 225 230 235 240 Thr Val Thr Lys Ala Thr Leu Ser Arg Asp Lys Lys Ser Val Glu Val 245 250 255 Val Val Asn Lys Pro Phe Thr Arg Asn Gln Glu Tyr Thr Ile Thr Ala 260 265 270 Thr Gly Ile Lys Asn Leu Lys Gly Glu Thr Ala Lys Glu Leu Thr Gly 275 280 285 Lys Phe Val Trp Ser Val Gln Asp Ala Val Thr Val Ala Leu Asn Asn 290 295 300 Ser Ser Leu Lys Val Gly Glu Glu Ser Gly Leu Thr Val Lys Asp Gln 305 310 315 320 Asp Gly Lys Asp Val Val Gly Ala Lys Val Glu Leu Thr Ser Ser Asn 325 330 335 Thr Asn Ile Val Val Val Ser Ser Gly Glu Val Ser Val Ser Ala Ala 340 345 350 Lys Val Thr Ala Val Lys Pro Gly Thr Ala Asp Val Thr Ala Lys Val 355 360 365 Thr Leu Pro Asp Gly Val Val Leu Thr Asn Thr Phe Lys Val Thr Val 370 375 380 Thr Glu Val Pro Val Gln Val Gln Asn Gln Gly Phe Thr Leu Val Asp 385 390 395 400 Asn Leu Ser Asn Ala Pro Gln Asn Thr Val Ala Phe Asn Lys Ala Glu 405 410 415 Lys Val Thr Ser Met Phe Ala Gly Glu Thr Lys Thr Val Ala Met Tyr 420 425 430 Asp Thr Lys Asn Gly Asp Pro Glu Thr Lys Pro Val Asp Phe Lys Asp 435 440 445 Ala Thr Val Arg Ser Leu Asn Pro Ile Ile Ala Thr Ala Ala Ile Asn 450 455 460 Gly Ser Glu Leu Leu Val Thr Ala Asn Ala Gly Gln Ser Gly Lys Ala 465 470 475 480 Ser Phe Glu Val Thr Phe Lys Asp Asn Thr Lys Arg Thr Phe Thr Val 485 490 495 Asp Val Lys Lys Asp Pro Val Leu Gln Asp Ile Lys Val Asp Ala Thr 500 505 510 Ser Val Lys Leu Ser Asp Glu Ala Val Gly Gly Gly Glu Val Glu Gly 515 520 525 Val Asn Gln Lys Thr Ile Lys Val Ser Ala Val Asp Gln Tyr Gly Lys 530 535 540 Glu Ile Lys Phe Gly Thr Lys Gly Lys Val Thr Val Thr Thr Asn Thr 545 550 555 560 Glu Gly Leu Val Ile Lys Asn Val Asn Ser Asp Asn Thr Ile Asp Phe 565 570 575 Asp Ser Gly Asn Ser Ala Thr Asp Gln Phe Val Val Val Ala Thr Lys 580 585 590 Asp Lys Ile Val Asn Gly Lys Val Glu Val Lys Tyr Phe Lys Asn Ala 595 600 605 Ser Asp Thr Thr Pro Thr Ser Thr Lys Thr Ile Thr Val Asn Val Val 610 615 620 Asn Val Lys Ala Asp Ala Thr Pro Val Gly Leu Asp Ile Val Ala Pro 625 630 635 640 Ser Glu Ile Asp Val Asn Ala Pro Asn Thr Ala Ser Thr Ala Asp Val 645 650 655 Asp Phe Ile Asn Phe Glu Ser Val Glu Ile Tyr Thr Leu Asp Ser Asn 660 665 670 Gly Asn Arg Leu Lys Lys Val Thr Pro Thr Ala Thr Thr Leu Val Gly 675 680 685 Thr Asn Asp Tyr Val Glu Val Asn Gly Asn Val Leu Gln Phe Lys Gly 690 695 700 Asn Asp Glu Leu Thr Leu Leu Thr Ser Ser Ser Thr Val Asn Val Asp 705 710 715 720 Val Thr Ala Asp Gly Ile Thr Lys Arg Ile Pro Val Lys Tyr Ile Asn 725 730 735 Ser Ala Ser Val Pro Ala Ser Ala Thr Val Ala Thr Ser Pro Val Thr 740 745 750 Val Lys Leu Asn Ser Ser Asp Asn Asp Leu Thr Phe Glu Glu Leu Ile 755 760 765 Phe Gly Val Ile Asp Pro Thr Gln Leu Val Lys Asp Glu Asp Ile Asn 770 775 780 Glu Phe Ile Ala Val Ser Lys Ala Ala Lys Asn Asp Gly Tyr Leu Tyr 785 790 795 800 Asn Lys Pro Leu Val Thr Val Lys Asp Ala Ser Gly Lys Val Ile Pro 805 810 815 Thr Gly Ala Asn Val Tyr Gly Leu Asn His Asp Ala Thr Asn Gly Asn 820 825 830 Ile Trp Phe Asp Glu Glu Gln Ala Gly Leu Ala Lys Lys Phe Ser Asp 835 840 845 Val His Phe Asp Val Asp Phe Ser Leu Ala Asn Val Val Lys Thr Gly 850 855 860 Ser Gly Thr Val Ser Ser Ser Pro Ser Leu Ser Asp Ala Ile Gln Leu 865 870 875 880 Thr Asn Ser Gly Asp Ala Val Ser Phe Thr Leu Val Ile Lys Ser Ile 885 890 895 Tyr Val Lys Gly Ala Asp Lys Asp Asp Asn Asn Leu Leu Ala Ala Pro 900 905 910 Val Ser Val Asn Val Thr Val Thr Lys 915 920 

What is claimed is:
 1. A host cell comprising at least two functional heterologous recombinant polypeptides, at least one of which is present as an s-layer structure in a support-bound form, and the polypeptides being located in each case in different compartments of the host cell.
 2. The cell according to claim 1, wherein the cell is a gram-negative bacterial cell.
 3. The cell according to claim 1, wherein the compartments are selected from the group consisting of cytosol, the outside and inside of the cytoplasmic membrane, the periplasmic space and the outside and inside of the outer membrane.
 4. The cell according to claim 1, wherein the cell is a eukaryotic cell.
 5. The cell according to claim 1, wherein the compartments are selected from the group consisting of cytosol, the outside and inside of the cytoplasmic membrane and cell organelles.
 6. The cell according to claim 1, wherein a plurality of the recombinant polypeptides are bound to a support.
 7. The cell according to claim 1, wherein the polypeptides in a support-bound form are present in the form of fusion polypeptides having support domains.
 8. The cell according to claim 1, wherein the polypeptides in a support-bound form are present in the form of S-layer structures, membrane-bound polypeptides and/or as components of recombinant phage structures.
 9. The cell according to claim 1, wherein the recombinant polypeptides are selected from the group consisting of enzymes, cytokines, antibody-binding proteins, DNA-binding epitopes, antigenic, allergenic and immunogenic epitopes and streptavidin.
 10. The cell according to claim 1 or 9, wherein the recombinant polypeptides are enzymes.
 11. The cell according to claim 10, wherein the enzymes catalyze a multistage enzymatic reaction.
 12. The cell according to claim 11, wherein the enzymes catalyze the synthesis of polyhydroxy-alkanoates.
 13. A recombinant bacterial ghost obtainable from a gram-negative cell according to claim 1, comprising at least two functional recombinant polypeptides bound to a support.
 14. A method for preparing a host cell according to claim 1, comprising the steps of (a) providing a host cell which has been transformed with at least two nucleic acids encoding polypeptides, at least one of which is linked to a sequence encoding a support domain in order to facilitate expression of the polypeptide in a support-bound form, and (b) culturing the host cell under conditions which induce expression of the polypeptides by the nucleic acids encoding the polypeptides.
 15. A vaccine comprising a host cell of claim 1 or a ghost of claim
 13. 16. An enzyme reactor comprising a host cell of claim 1 or a ghost of claim
 13. 